A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751331



Internal ID21388850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234776254..234783253hg38UCSC Ensembl
chr1:234912001..234919000hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433071
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751331
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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